5&#39;,6&#39;-dihydro-2h-pyran-4&#39;-yl ethers of anabolic steroids



United States Patent US. Cl. 260-23955 36 Claims ABSTRACT OF THE DISCLOSURE The ',6-dihydro-2H-pyran-4'-yl ethers of anabolic steroids have high oral activities.

This is a continuation-in-part of US. Pat. application Ser. No. 731,000 filed May 22, 1968.

This invention relates to novel and useful 5',6'-dihydro- 2H-pyran-4'-yl ethers of anabolic steroids, the steroid nucleus thus bearing a new group represented by the formula:

In the preferred embodiment, this new group is added at the C-3, 0-175 or C-3,17p positions of the steroid nucleus.

The preferred anabolic steroidal ethers of this invention have the formulas:

ice

R1 v Rn ---R12 "-Rz2 R13 v l/ Xa- Xa= Z RID/R20 4 V VI) wherein:

R R11 R R 5, R and R each is hydrogen or methyl (preferably one of R and R is methyl);

R 2 is hydrogen or lower alkyl;

R is hydrogen or chloro;

R is lower alkyl or lower cycloalkyl;

R is methyl or ethyl;

R R and R each is hydrogen, methyl, fiuoro, or hloro; and R is not present when 2., is a double bond;

X is keto or a-hydrogen together with fi-X, ,B-hydrogen, or fl-hydroxy, and conventional hydrolyzable esters thereof;

X is X, hydroxy, or conventional hydrolyzable esters thereof; and at least one of X and X is X; and

Z and Z each is a single bond or double bond.

The term anabolic steroids is used herein to denote androstanes and 19-norandrostanes having anabolic activity. The preferred anabolic steroids have 5',6'-dihydro- 2I-I-pyran-4-yloxy groups at positions C-BB, 0-1713, or C3fi,17;8 of the steroid nucleus.

The compounds represented by Formulas I-VI are anabolic agents with a favorable anaboliczandrogenic ratio, also possess anti-estrogenic," anti-gonadotrophic, and anti-fibrillatory activities, and can be used in the same manner as testosterone. These compounds are administered by the usual routes, whether orally or parenterally, either alone or in conjunction with other medicinalagents, or in pharmaceutically acceptable, non-toxic compositions formed by the. incorporation of any of the normally employed excipients.

The terms (lower)alkyl and derivations thereof appearing in the above definitions and elsewhere in the instant specification denote alkyl groups containing from one to six carbon atoms, inclusive, such as methyl, ethyl, propyl, isopropyl, butyl, isobutyl, t-butyl, pentyl, amyl, hexyl, and the like.

The term conventional hydrolyzable ester as used herein denotes those hydrolyzable ester groups conventionally employed in the steroid art, preferably those hydrocarbon carboxylic acids or phosphoric acids and their salts. The term hydrocarbon carboxylic acid defines both substituted and unsubstituted hydrocarbon carboxylic acids. These acids can be completely saturated or possess varying degreesof unsaturation (including aromatic), can be of straight chain, branched chain, or cyclic structure, and preferably contain from one to 12 carbon atoms. In addition, they can be substituted by functional groups, for example, hydroxy, alkoxy containing up to six carbon atoms, acyloxy containing up to 12 carbon atoms, nitro, amino, halogeno, and the like, attached to the hydrocarbon backbone chain. Typical conventional hydrolyzable esters thus included within the scope of the term and the instant invention are acetate, propionate, butyrate, valerate, caproate, enanthate, caprylate, perlargonate, acrylate, undecenoate, phenoxyacetate, benzoate, phenylacetate, diphenylacetate, diethylacetate, trimethylacetate, t-butylacetate, trimethylhexanoate, methylneopentylacetate, cyclohexylacetate, cyclopentylpropionate, adamantoate, glycolate, methoxyacetate, hemisuccinate, hemiadipate, hemi-pLB-dimethylglutarate, acetoxyacetate, 2-chloro-4-nitrobenzoate, aminoacetate, diethylaminoacetate, piperidinoacetate, fi-chloropropionate, trichloroacetate, p-chlorobutyrate, dihydrogen phosphate, dibenzyl phosphate, benzyl hydrogen phosphate, sodium benzyl phosphate, cyclohexylamrnonium benzyl phosphate, sodium phenyl phosphate, sodium ethyl phosphate, di-p-nitrobenyl phosphate, sodium o-methoxyphenyl phosphate, cyclohexylammonium p-cyanobenzyl phosphate, sodium phenacyl phosphate, benzyl o-carbomethoxyphenyl phosphate, and the like.

By the term aryl are included aryl, aralkyl, and alkaryl groups, such as phenyl, p-chlorophenyl, pmethoxyphenyl, benzyl, phenethyl, tolyl, ethylphenyl, and the like. The wavy line (2) designates and includes both the alpha and beta configurations.

The novel 17fi-(5',6' dihydro 2H pyran-4'-yloxy) ethers of Formulas I, H, III, and IV can be prepared from the corresponding 17B-hydroxy compounds by a process which can be illustrated schematically as follows:

In these formulas, 10 11 12 13, 14 15 16, 17 R R and X have the meanings given above with respect to Formulas I-IV.

In carrying out the above illustrated process, the 17,8- hydroxy compounds (I, II, III, and IV) are reacted under substantially anhydrous conditions with an excess of 4-(lower)alkoxy-5,6'-dihydro-2H-pyran, preferably 4-methoxy-5-6'-dihydro-2H pyran. The hydroxy compounds are reacted, for example, with from about two to about 50 or more molecular equivalents for each hydroxyl group in the steroid starting material, in the presence of a small amount of an acidic catalyst, such as hydrochloric acid, p-toluenesulfonic acid, boron trichloride etherate, and the like, either alone or together with an inert, organic solvent, such as benzene, diethyl ether, methylene chloride, or the like, at a temperature ranging from about 0 C. to about C. (preferably at around room temperature, i.e., 25 C.) for about five minutes to about 48 hours, thus giving the corresponding 17,3-(5',6'-dihydro-2H-pyran-4-yl) ethers represented by Formulas I-IV. In carrying out this reaction, a second series of ethers corresponding to those represented by the formulas but wherein X is 4-methoxytetrahydropyran-4'-yloxy are also formed. Use of hydrocarbon solvents for the reaction medium, higher catalyst concentrations, and longer reaction times increase the yield of the 5',6'-dihydro-2H-pyran-4'-yloxy compounds.

The 3-, and 3,17fi-bis(5',6'-dihydro-2H-pyran-4'- yl) ethers represented by Formulas V and VI can be prepared from the corresponding androst-4-en-l7fi-o1-3- one and 19-norandrost-4-en-175-ol-3-one compounds by a process which can be illustrated schematically as follows:

Il -R12 In these formulas, R R R R R X, and Z have the meanings given with respect to Formulas V and VI above, and R is an alkyl, alkenyl, cycloalkenyl, or cycloalkyl group having up to 12 carbon atoms.

In carrying out the above-illustrated .process, 170;- methylandrost-4-cn-l7 3-ol-3-one, for example, (XVII: R and R =hydrogen; R R and R =methyl) is reacted under substantially anhydrous conditions with an excess of 4'-(1ower)alkoxy-5,6-dihydro-2H-pyran, preferably 4-methoxy-5,6-dihydro-2H-pyran, as described above with respect to Formulas I-IV to give the corresponding 17a methyl 17,8 (5',6-dihydro-2H-pyran-4'- yloxy)-androst-4-en-3-one (XVIII). This compound can be converted to the 3fi-hydroxy derivative by dissolving it in an inert solvent such as a (lower)alkanol, such as methanol, and ether, such as dioxane or tetrahydrofurane or the like, and reacting it under neutral conditions with a metal hydride, such as lithium tri-t-butoxy aluminum hydride, at temperatures ranging from room temperature to reflux temperature for from about one hour to about 24 hours, thus giving the corresponding l7a-methyl-l7f1- (5',6' dihydro 2H pyran 4-yloxy)androse-4-en-313-ol (XIX). To obtain the 3B-ester of Formula XX, the prodnot can be reacted with an organic acid anhydride in pyridine or with a solution of ethyl-magnesium bromide and the desired organic chloride in anhydrous ether; for example, reaction with acetic anhydride yields 3fl-acetoxy- 17a methyl 175 (5,6'-dihydro-2H-pyran-4'-yloxy)androst-4-ene (XX: R -=methyl). By this procedure, the compounds represented by Formulas XVIII-XX are obtained with other androst-4-en-l7 3-ol-3-ones wherein R is hydrogen or lower alkyl; R is hydrogen or methyl;

(XXII) E Z4 Rm R20 (XXIII) R is ethyl or methyl; and R and R each is hydrogen, methyl, ffuoro, or chloro.

In carrying out the above-illustrated proces to form the 3p-(5',6'-dihydro-2H-pyran-4'-yl) ethers of Formulas XII and XXIII from the compounds represented by Formula XVII, the keto group at C-3 is first reduced to 3 3-hydroxy such as by reaction with lithium tri-t-butoxy aluminum hydride as described above with respect to Formula XIX to yield, for example, 17a-methylandrost-4-ene-3B,17B- diol. The product is then esterified with one molar equivalent of acetic anhydride by procedures described with respect to Formula XX to form a mixture of mono-esters. The 17fi-acetoxy compounds are separated from the mixture by conventional chromatographic techniques. For example, 17a-methylandrost-4-en-17/3-ol-3-one (XVII: R R and R =methyl; R and R =hydrogen) is reduced to 17a-methylandrost-4-ene-3p,17,8-diol and the product is esterified to form 17u-methyl-17/3-acetoxyandrost-4-en- 3 8-01 (XXI). This compound is then reacted with 4'- (lower)-alkoxy-5', 6-dihydro-2H-pyran as described above with respect to Formula XVIII to yield the corresponding 3,3 ether, for example, 3 8 (5,6' dihydro-2H-pyran-4'- yloxy) 17a-methyl-17 8-acetoxyandrost-4-ene (XXII). If the 17,3-hydroxy compound as described in Formula XXIII is desired, the latter product is hydrolyzed by conventional procedures, for example, in a solution of potas sium hydroxide in methanol, to yield the desired product, for example, 36 (5',6' dihydro-2H-pyran-4'-yloxy)-17(xmethylandrost 4 en-l7B-ol. By this procedure other 313- (5,6'-dihydro-2H-pyran-4'-yloxy) compounds represented by Formulas XXII and XXIII can be prepared from the corresponding compounds of Formula XVII wherein R 7 is hydrogen or lower alkyl; R is hydrogen or methyl; R is methyl or ethyl; and R and R each is hydrogen, methyl, fiuoro, or chloro.

In the above-illustrated processes to make the 36,175- bis (',6-dihydro-2H-pyran-4'-yloxy) ethers represented by Formula XXIV, the corresponding 17/3-hydroxy-3-keto of Formula XVII is first reduced by reaction with a metal hydride, such as lithium tri-t-butoxy aluminum hydride, to yield the corresponding 3/3-hydroxy compound as described above with respect to the compounds of Formula XIX. The 35,17/3-dihydroxy compound, for example, 170:- methylandrost-4-ene-3fl,17/3-diol, is then reacted with a molar excess of 4'-(lower)alkoxy-5,6'-dihydro-2H-pyran as described above with respect to Formula XVIII to yield the corresponding 3 3,175 bis(5',6'-dihydro-2H-pyran-4'- yloxy) ether, such as, for example, 3B,17/i-bis(5',6'-dihydro 2H pyran-4'-yloxy)-17a-methylandrost-4-ene. By this procedure, other compounds represented by Formula XXIV, wherein R R R R R and X are as defined above, can be obtained from the corresponding substituted compounds represented by Formula XVII.

By the above-illustrated procedures, the 35-, 175-, and 3,1718 bis(5,6' dihydro 2H-pyran-4-yloxy)-19-norandrosta-4,9()-dienes represented by Formula VI can be prepared from the corresponding 19-norandrosta-4,9( 10)- dien-17fl-ol-3-ones.

The 4'-(lower)alkoxy-5',6'-dihydro-2H-pyran reactants used to form the ethers of this invention can be prepared by well-known methods. For example, tetrahydro-4-pyrone can be reacted with a primary or secondary lower alkanol under acidic conditions to form the intermediate, 4,4'-di- (lower)alkoxytetrahydropyran, which upon distillation with an acid, such as toluenesulfonic acid or mestylenesulfonic acid, yields the 4'-(l0wer)alkoxy-5',6'-dihydro- 2H-pyran product. Such a method is described by Reese et al., J. Am. Chem. Soc. 89, 3367 (1967). The lower alkanol is preferably methanol but it can be other lower alcohols, such as ethanol, propanol, isopropanol, butanol, isobutanol, pentanol, amyl alcohol, hexanol, and the like, to form the corresponding pyrans, such as, for example, 4' methoxy-S,6-dihydro-2H-pyran, 4'-ethoxy-5',6-dihydro-2H-pyran, etc.

The ethers of Formula I are prepared from known 19- norandrostan 17 ol 3-ones and androstan-17-ol-3-ones containing the substituents represented by R R R and R See, for example, JACS 81, 428 (1959) JACS 76, 5024 (1954); and US. Pats. 2,756,244 and 2,844,602.

In preparing the ethers of Formula II, the substituents R12, R R and R are likewise present in the known starting steroids. See, for example, Lo Sperimentale 106, 490 (1956); J. Org. Chem. 21, 1432 (1956); JACS 80, 4717 (1959); L0 Sperimentale 104, 490 (1956); Tetrahedron 3, 14 (1958); JACS 75, 5366 (1953); and US. Pats. 3,028,401 and 3,213,986.

In preparing the ethers of Formula III, the substituents R R R and R are also present in the known starting steroids. See, for example, US. Pat. 3,067,214.

In preparing the ethers of Formula IV, the substituents R R and R are present in the known starting compounds and can be obtained from known compounds by conventional techniques. See, for example, Int. Steroid Congress, Milan, p. 68 (1962); JACS 82, 5494 (1960); German Pat. No. 1,096,356; and US. Pat. No. 3,361,774.

In preparing the ethers of Formula V, the substituents R R R R and R are present in the known starting compounds. See, for example, JACS 80, 4717 (1958); JACS 83 4663 (1961); J. Pharm. Pharmacol 9, 929 (1957); Ber 71, 1024 (1938); Endocrinology 65, 265, and US. Pats. 3,028,401, 3,047,592, 3,052693 and 3,067,214.

In preparing the ethers of Formula VI the substituents R and R are also present in the known starting compounds. See, for example, JACS 83, 4463 (1961); J. Chem. Soc., 4472 (1964); and US. Pat. 3,086,027, 3,248,294 3,250,793, and 3,257.278.

8 Starting materials having an 18-methyl group (R ethyl) are obtainable by methods described by Smith et al. in Experimenta, vol. 19, pages 394-396 (1963).

This invention is further illustrated by the following specific but non-limiting examples.

EXAMPLE 1 To a solution of 1 g. of 5a,19-norandrost-17fi-o1-3-one and 25 cc. of benzene there is added 2 cc. of 4'-methoxy- 5,6'-dihydro-2H-pyran. Next, approximately 5 cc. of the mixture of benzene and dihydropyran is distilled off to remove moisture, and the remaining mixture is then cooled to room temperature. To the cooled mixture is then added 0.1 g. of p-toluenesulfonic acid, and the resulting reaction mixture is held at room temperature for 72 hours. Following this reaction period, the reaction mixture is washed with an aqueous 5% sodium carbonate solution and then with water until a neutral pH is obtained, then dried over anhydrous sodium sulfate and evaporated to dryness. The dry residue is then chromatographed by passing it, dissolved in hexane, through a column of neutral alumina, to yield 17fi-(5',6-dihydro- 2H-pyran-4-yloxy)-5a,19-norandrost-3-one.

EXAMPLE 2 By repeating the procedure of Example 1 in every detail but one, namely, replacing the 5a-19-I10I21I1df08t- -o1-3-one with:

EXAMPLE 3 Repeating the procedure of Example 1 in every detail but one, namely, replacing 5a,19-norandrost-17-ol-3-one with: androst-4'en-17fi-ol-3-one, 17u-methylandrost-4-en-17B-ol-3-one, 17a-ethyl-androst-4-en-17fl-ol-3-one, 17a-propylandrost-4-en-17B-ol-3-one, 7a-methlylandrost-4-en-17/3-01-3 -one, 4-chloroandrost-4-en-17/i-0l-3-one, 19-norandrost-4-en-17-ol-3-one, 17a-methyl-19-norandrost-4-en-17-01-3-one, 17a-ethyl-19-norandrost-4-en-17-ol-3-one, 17a-propyl-19-norandrost-4-en-17-ql-3-one, 7ot-methyl-19-norandrost-4-en-17-ol-3-one, 7a,17a-dimethyl-19-norandrost-4-en-17 3-ol-3-one, and 4-chloro-19-norandrost-4-en-17-o1-3-onethe correspondmg 175-(5',6'-dihydro-2I-I-pyran-4-yloxy)androst- 4-en-3-ones and 19-norandrost-4-en-3-ones are obtained, e.g., 175- 5 ',6'-dihydro-2H-pyran-4'-yloxy) androst-4en- 3-one, 17a-methy1-17fi-(5,6'-dihydro-2H-pyran-4-yloxy) androst-4-en-3-one, 17ot-ethyl-17,8 (5',6-dihydro-ZH-pyran-4-yloxy) androst-4-en-3-0ne,

6a-methyl-17B- (,6'-dihydro-2H-pyran-4-yloxy)- l9- norandrost-4-en-3-one,

1713-(5',6-dihydro-2H-pyran-4'-yloxy) 19-norandrost- 4-en-3-one,

17B- (5',6'-dihydro-2H-pyran-4'-yloxy) -18-methyl-19- norandrosta-4,6-dien-3-one,

17a,18-dimethyl-17fl(5,6'-dihydro-2H-pyran-4'-yloxy)- 19-norandrosta-4,6-dien-3-one,

60,17a,18-trimethyl-17B-(5,6'-dihydro-2H-pyran-4'- yloxy)- 19-norandrosta-4,6-dien-3-one,

6a,l-8-dimethyl-17a-ethyl-17fl- (5',6'-dihydro-2H-pyran- 4-yloxy) -19-norandrosta-4,6-dien-3-one,

6a, 1 7a-dimethyl-17 8-(5',6-dihydro-2H-pyran-4'-yloxy) 19-norandrostra-4,6-dien-3-one,

6u-methyl- 175- 5 ',6-dihydro-2H-pyran-4-yloxy -19- norandrosta-4,6-dien-3-one,

6a-fluoro-17a,18-dimethyl-l7fi-(5,6'-dihydro-2H-pyran- 4'-yloxy) -19-norandrost-4-ene-3-or1e, and the like.

EXAMPLE 7 A solution of 1 g. of 17fl-(5',6'-dihydro-2H-pyran-4'- yloxy)-19-norandrost-4-ene-3-one in 50 ml. of tetrahydrofuran is added over a 30-minute period to a stirred suspension of 1 g. of lithium tri-t-butoxy aluminum hydride in 50 ml. of anhydrous tetrahydrofuran and this mixture is heated at reflux for two hours. To the mixture are cautiously added 5 ml. of ethylacetate and 2 ml. of water. Sodium sulfate is next added, the mixture is filtered, and the solid thus collected is washed with hot ethylacetate. The combined organic solutions are then evaporated to yield 17,8-(5',6-dihydro-2H-pyran-4'-yloxy)-19 norandrost-4- en-Bfi-ol which may be further purified through recrystallization from acetone :hexane.

Similarly, repeating this procedure with other products of Example 6 yields the corresponding 3fi-hydroxy derivatives, e.g.,

1 2. 6a-methyl- 17 ,3- (5 ',6-'-dihydro-2H-pyran-4'-yloxy) -19- norandrost-4-en-3fi-ol, 17/3- 5 ',6'-dihydro-2H-pyran-4'-yloxy) -19-nora.ndrost-4- en-3B-ol, 17(3-( 5 61-dihydro-2H-pyran-4f-y1oxy)-18'-me qhyl- 19- norandrosta-4,6-dien-3 [3-01, 17a,18-dimethyl-17B-(5,6'-dihydro-2H-pyran-4'- yloxy) 19-norandrosta-4,6-dien-35-01, 6a,17a,18-trimethyl-17fi-(5',6-dihydro-2H-pyran-4'- yloxy)-19-norandrosta-4,6-dien-318-01, 6a,18-dimethyl-17a-ethyl-17p-(5,6'-dihydro-2H-pyra.n-

4-yloxy) -19-r1orandrosta-4,6-dien-3/8-ol, 6a,17a-dimethyl-17;3-(5,6-dihydro-2H-pyran-4'- yloxy 19 norandrosta-4,6-dien-3 5-01, 6a-methyl1 7 3- 5 6-dihydro-ZH-pyrarMK-yloxy -19- norandrosta-4,6-dien-318-01, and the like.

EXAMPLE 8 A mixture of 1 g. of 17; -(5',6-dihydro-2H-pyran-4- yloxy)-19-norandrost-4-en 3 8 ol, 4 m1. of pyridine, and 2 ml. of acetic anhydride is allowed to stand at room temperature for 15 hours. The mixture is then poured into ice water and the solid which forms is collected by filtration, washed with water, and dried to yield Bfi-acetoxy- 17fl-(5',6'-dihydro-2H-pyran-4'-yloxy)-l9 norandrost 4- ene which may be further purified through recrystallization from acetone:hexane.

Similarly, repeating this procedure with other products of Example 7 yields the corresponding 3fi-acetoxy derivatives, e.g.,

3 B-acetoxy- 17 a-methyl- 17 8- 5 ,6'-dihydro-2H-pyran-4'- yloxy) androst-4-ene,

3 fl-acetoxy- 1 7 a-ethyl- 17 8- (5 ,6 '-dihyd ro-2H-pyran-4'- yloxy) 1 8-methylandrost-4-ene, and the like.

EXAMPLE 9 Repeating the procedure of Example 7 but replacing:

19-norandrost-4-en-17;8-o1-3-one19-norandrost 4 ene- 3 5,17B-diol is obtained.

A mixture of 1 g. of l9-norandrost-4-ene-3fl,17fi-diol, 4 ml. of pyridine, and 2 ml. of acetic anhydride is allowed to stand at room temperature for 15 hours. The mixture is then poured into ice water, and the solid 'which forms is collected by filtration, washed with water, and dried. The mixture is chromatographed on neutral alumina, eluting with etherzhexane, to yield 17,8-acetoxy-19 norandrost-4- en-3fi-ol.

Repeating this sequence of procedures with other 19- norandrost-4en-17p-ol-3-ones, androst 4 en-17p-ol-3- ones, 19 norandrosta 4,6 dien-17fl-ol-3-ones, and androsta 4,6 dien l7p-ol-3-ones having hydrogen, methyl, chloro, or fiuoro groups at C6oz and/ or C6 8 (at C6 with 4,6-dienes); hydrogen and lower alkyl groups at Cl7oc; and hydrogen or methyl groups at C18 yields the corresponding 35 hydroxy-17a-ester compounds, e.g.,

l75-acetoxy-18-methy1androst-4-en-35-01, 17u,18-dimethyl-17 8-acetoxyandrost-4-en-3/3-ol, 17a-ethyl-17fi-acetoxy-18-methylandrost-4-en-318-01, 17a-methy1- 17 S-acetoxyandrost-4-en-3 5-01, 17 methyl-17 fl-acetoxyandrost-4-en-3p-ol, -acetoxyandrost-4-en-35-01, l7fl-acetoxy-18-methylandrosta-4,6-dien-3 19-01, 17a,1S-dimethyl-17,8-acetoxyandrosta-4,6-dien-3B-ol, 17a-ethyl-17 3-acetoxy-18-methylandrosta-4,6-

dien-Sfi-ol, Not-methyl-17,8-acetoxyandrosta-4,6-dien-3,6-ol, 17a-ethyl-17,6-acetoxyandrosta-4,6-dien-3p-ol, 17p-acetoxyandrosta-4,6-dien-3p-ol, and the like.

13 EXAMPLE 10 Repeating the procedure of Example 1 but replacing oz,19 norandrost-l7B-ol-3-one with 17;3 acetoxy-19- norandrost 4 en-3fi-o1-3 8 (5,6-d ihydro-2H-pyran- 4' xyloxy)-17 8-acetoxy-19-n0randrost };ene is obtained. Similarly, substituting the other products of Example 9 in this procedure yields the corresponding'iip-ethers, e.g.,

3 p- 5 ',6'-dihydro-2H-pyran-4yloxy) 17fi-acetoxyl8-methylandrost-4-ene,

35-(5',6'-dihydro-2H-pyran 4'-yloxy)-17a,18-dimethyl- 17 B-acetoxyand rost-4-ene,

3 ,8- 5 '6-dihydro-2H-pyran-4'-yloxy) -l7p-acetoxyandrost-4-ene,

3 3-( 5 6'-dihydro-2H-pyran-4'-yloxy) -17;9-acetoxyacetoxy-8-methylandrost-4,6-diene,

3 8- 5',6'-dihydro-2H-pyran-4'-y1oxy -l7a,1 8-dimethyl- 17 B-acetoxyandrosta-4,6-diene,

3 B- 5 ,6-dihydro-2H-pyran-4-yloxy 17a-ethyl- 17,8-

acetoxy-18-methylandrosta-4,6-diene,

3 ,8- 5 ',6'-dihydro-2H-pyran-4'-yloxy -l7u-methyl 17 B-acetoxyandrosta-4,6-diene,

35- 5 ',6-dihydro-2H-pyran-4'-yloxy) -17a-ethyll7;3-acetoxyandrosta-4,6-diene,

3 ,8- 5 ',6-dihydro-2H-pyran-4'-yloxy) -1 7 8-acetoxyandrosta-4,6-diene,

3 B- 5 ',6'-dihydrQ-ZH-pyran-4-yloxy) -17;9-acetoxy- 1S-methyl-19-norandrost-4-ene,

35- 5,6'-dihydro-2H-pyran-4'-y1oxy) 17a, l8-dimethyll7B-acetoxy-19-norandrost-4-ene,

3 fl- (5 ,6'-dihydro-2H-pyran-4'-yloxy) l7a-ethyl- 17ftacetoxy-lS-methyl-19-norandrost-4-ene,

3 p- 5 ',6-dihydro-2H-pyran-4'-yloxy) -17a-methyl- 17fl-acetoxy-19-norandrost-4-ene,

3 [i- 5 ',6-dihydro-2H-pyran-4-yloxy) 17B-acetoxy- 19-norandr0st-4-ene,

3 18- 5 ,6-dihydro-2H-pyran-4'-yloxy) -17/3-acetoxyl8-methyl-19-norandrosta-4,6-diene,

3/3-(5',6'-dihydro-2H-pyran-4'-yloxy)-17a,18-dimethyl-17/8-acetoxy-19-norandrosta-4,6-diene,

3,3-(5',6'-d.ihydro-2H-pyran-4'-yloxy) -17a-ethyl-17[3- acetoxy-l S-methyl-19-norandrosta-4,6-diene,

3 B- 5',6'-dihydro-2H-pyran-4'-yloxy -17a-ethyll7fi-acetoxy-19-norandrosta-4,6-diene,

3 ;8-( 5',6-dihydro-2H-pyran-4'-yloxy -17;9-acetoxy- 19-norandrosta-4,6-diene, and the like.

EXAMPLE 11 A solution of 1 g. of 3/3-(5',6-dihydro-2H-pyran-4'- yloxy) 17a-methyl-17fi-acetoxy-l9-norandrost 4 ene in 50 ml. of methanol is heated at reflux for three hours with a solution of potassium hydroxide in 1 ml. of water. The reaction mixture is then poured into ice water and the solid which forms is collected by filtration, washed with water to neutrality, and dried to yield 3 3- (5',6' dihydro 2H-pyran-4'-yloxy)-17a-methyl-19-norandrost 4-en-17B-ol which is recrystallized from methylene chloridezether.

Similarly, the other 17/8ester products of Example are converted to the corresponding 17fl-ols by this procedure.

EXAMPLE 12 Repeating the procedure of Example 7 but replacing 17oz ethynyl 17 8-(5',6'-dihydro-2H-pyran-4'-yloxy)- 19 norandrost-4-en-3-one with 17m methyl 19-norandrost-4 en-17fi-ol--3-one-17a-rnethyl-l9-norandrost- 4-ene-3;3,17B-diol is obtained. Then repeating the procedure of Example 1 but replacing 5a,19-norandrost-17B- ol-3-one with 17oz methyl l9-norandrost-4-en-3B,17B- diol and using 4 m1. instead of 2 ml. of 4-methoxy-5,6'- dihyd'ro-Z-H-pyran-3fl,17B-bis(5',6' dihydro-2H-pyran- 4'-yloxy)-17a-methyl-19-norandrost-4-ene is obtained.

Repeating this sequence of procedures with other 19- norandrost 4 en-17f3-ol-3-ones, androst 4 en-l7p-ol- 3-ones, 19 norandrosta-4,6-dien-l7fi-ol-3-ones, and androsta 4,6-diene-17p-o1-3-ones having hydrogen, methyl, chloro, or fluoro groups at C-6oc and/ or C-6fl positions (at 0-6 with 4,6-dienes); hydrogen and lower alkyl groups at C17oc; and hydrogen or methyl at 0-18 yields the corresponding 3B,17fl-bisethers, e.g., 3fl,17fl-bis(5',6- dihydro 2H pyran 4'-y1oxy)-17u-methylandrost-4- ene, 35,1718 bis(S',6'-dihydro 2H-pyran-4'-yloxy)-17a, 1S-dimethyl-19-norandrost-4 ene, and the like.

EXAMPLE 13 Repeating the procedure of Example 1 but replacing 5a,19-norandrost-17fi-ol-3-one with 19 norandrosta-4,9- (10) dien-1713-01-3-one17B-(5',6'-dihydro-2H-pyran-4'- yloxy)-l9norandrosta-4,9(10)-dien-3-one is obtained.

Similarly, repeating this procedure with other 19- norandr0sta-4,9(l0)-dien-17/3-01 3 ones and 19-norandrosta-4,9(10),11-trien-17B-ol-3-ones having hydrogen and lower alkyl groups at 0-170; yields the corresponding 17B- (5',6'-dihydro-2H-pyran-4-yloxy) compounds, e.g.,

17a-propyl-l7B-(5,6'-dihydro-2H-pyran-4-yloxy)-l 8- methyl-19-norandrosta-4,9( lO)-dien-3-one,

1718- 5',6-dihydro-2H-pyran-4'-yloxy)- l9-norandrosta- 4,9(10)-dien-3-one,

17 ,B- (5 ,6'-dihydro-2H-pyran-4'-yloxy)- l 8-methyl- 19- norandrosta-4,9(10)-dien-3-one,

17m-methy1-17/3-(5,6-dihydro-2H-pyran-4-yloxy)-19- norandrosta-4,9(10)-dien-3-one,

17a,18-dim ethyl--(5',6'-dihydro-2H-pyran-4-yloxy)- 19-norandrosta-4,9(10)-dien-3-one,

17 a-ethyll7 3-(5 ,6-dihydro-2H-pyran-4-yloxy)- 19- norandrosta-4,9(10)-dien-3-one,

l7a-ethyl-17,8-(5',6-dihydro-2H-pyran-4'-yloxy)-18- methyll9-norandr0sta-4,9( 1 0)-dien-3 -one,

17p-(5,6'-dihydro-2H-pyran-4'-yloxy)-18-methyl-19- norandrosta-4,9(10),1 1-trien-3-one,

17a-methyll 718-(5',6'-dihydro-2H-pyran-4'-yloxy)-19- norandrosta-4,9( 10), 1 l-trien-3-one,

17 a, l 8-dimethyl-17B-(5 ',6'-dihydro-2H-pyran-4'-yloxy)- 19-norandrosta-4,9(10),1 1-trien-3-one,

17u-ethyl-l7 B- (5 6'-dihydro-2H-pyran-4'-yloxy) -1 8- methyl-l9-norandrosta-4,9(10),1 1-trien-3-one,

17u-ethyl-l713-(5',6-dihydro-2H-pyran-4'-yloxy)-l9- norandrosta-4,9(10),1 1-trien-3-one,

17u-pr0pyl-17/3-(5,6-dihydro-2H-pyran-4"yloxy)-1 8- methyl-l9-norandrosta-4,9(10),1 l-trien-3-one,

17a-propyl- 175-(5',6-dihydro-2H-pyran-4-yloxy)- 19- norandrosta-4,9(10),-1 l-trien-3-one, and the like.

EXAMPLE 14 A solution of 1 g. of 17,8-(5',6'-dihydro-2H-pyran-4- yloxy)-19-norandrosta-4,9(10)-dien-3-one in 50 ml. of tetrahydrofuran is added over a 30-minute period to a stirred suspension of 1 g. of lithium tri-t-butoxy aluminum hydride in 50 ml. of anhydrous tetrahydrofuran and this mixture is heated at reflux for two hours. To the mixture are cautiously added 5 ml. of ethylacetate and 2 ml. of water. Sodium sulfate is next added, the mixture is filtered, and the solid thus collected is washed with hot ethylacetate. The combined organic solutions are then evaporated to yield 17;8-(5,6-dihydro-2H-pyran-4'-yloxy)-l9- norandrosta-4,9( 10)-dien-3 13-01 which may be further purified through recrystallization from acetone:hexane.

Similarly, repeating this procedure with other products 1 5 of Example 13 yields the corresponding 3 3-hydroxy derivatives, e.g., 17a-propyl-17,9-(5,6-dihydro-2H-pyran-4'-yloxy)-18- methyl-19-norandrosta-4,9(10)-dien-3 5-01, 17,3-(5,6-dihydro-2H-pyran4'-yloxy)-l9-norandrosta- 4,9(1 )-dien-3fi-ol, 17fi-(5',6-dihydro-2H-pyran-4'-yloxy)-1S-methyl-19- norandrosta-4,9(10)-dien-3i3-ol, 17a-methyl-l7,8-(5'6'-dihydro-2H-pyran-4'-yloxy)-19- norandrosta-4,9(10)-dien-35-ol, 17a,l8-dimethyl-17,8-(5',6-dihydro-2H-pyran-4-yloxy)- l9-norandr0sta-4,9(10)-dien-3fi-ol, 17aethyl-175-(56-dihydro-2H-pyran-4'-yloxy)-19- norandrosta-4,9(10)-dien-3fl-ol, 17a-ethyl-17 8-(56'-dihydro-2H-pyran-4'-yloxy)-l 8- methyl-19-norandrosta-4,9(10)-dien-3 -01, 17,8-(5',6'-dihydro-2H-pyran-4'-yloxy)18-methyl-l9- norandrosta-4,9(),1 1-trien-3 5-01, 17,9-(5,6'-dihydro-2H-pyran-4-yloxy)-19-norandrosta 4,9(10),11-trien-3 8-ol, 17a-methyl-17,6-(5',6-dihydro-2H-pyran-4-yloxy)-19- norandrosta-4,9(l0),l l-trien-3 3-01, 17a,18-dimethyl-17p-(5',6-dihydro-ZH-pyran-4'-yloxy)- l9-norandrosta-4,9(10),l 1-trien-3B-ol, 17a-ethyl-17,3-(5,6'-dihydro-2H-pyran-4-yloxy)-18- methyl-l9-norandrosta-4,9(l0),1 l-trien-3fl-ol, 17a-ethyl-17,8-(5',6'-dihydro-2H-pyran-4'-yloxy)-19- norandrosta-4,9(10),11-trien-3p-ol, 17a-pr0pyl-l7,8-(5',6'-dihydro-2H-pyran-4'-yloxy)-18- methyl-19-norandrosta-4,9(10),11-trien-3 3-ol, 17a-propyl-17f)-(5',6-dihydro-2H-pyran-4-yloxy) -19- norandrosta-4,9 10) ,1 l-trien-Bfi-ol, and the like.

EXAMPLE A mixture of 1 g. of 17,3-(5',6'-dihydro-2H-pyran-4'- yloxy) 19 norandrosta 4,9(10) dien-313-ol, 4 ml. of pyridine, and 2 m1. of acetic anhydride is allowed to stand at room temperature for 15 hours. The mixture is then poured into ice water and the solid which forms is collected 'by filtration, washed with water, and dried to yield 3fl-acetoxy 17,8 (5',6'-dihydro-2-H-pyran-4'-yloxy)-l9- norandrosta-4,9(1'0)-diene which may be further purified through recrystallization from acetonezhexane.

Similarly, repeating this procedure with other products of Example 14 yields the corresponding 3fi-acetoxy derivatives, e.g.,

3fl-acetoxy-17a,1'8-dimethyl-17,9- (5',6-dihydro-2H- pyran-4'-yloxy) -19-norandrosta-4,9 10 -dien, 3fl-acetoxy-17a-ethyl-17fl-(5, 6'-dihydro-2H-pyran-4'- yloXy)-19-norandrosta-4,9 10)-dien, 3fi-acetoxy-17a-propyl-17f3- (5 ',6'-dihydro-2H-pyran-4'- yloxy)-1 S-methyll 9-norandrosta-4,9(10), l l-triene, and the like.

EXAMPLE 16 Repeating the procedure of Example 14 but replacing:

175%5',6'-dihydro-2I-I-pyran-4'-yloxy) 19-norandrost-4- en-3-one with 19-norandrosta-4,9(l0)-dien 17,8 01-3- one-l9-norandrosta 4,9(10)-diene-3fi,17,8-diol is obtained.

A mixture of 1 g. of l9norandrosta4,9(10)-diene-3fl, 175-diol, 4 ml. of pyridine, and 2 ml. of acetic anhydride is allowed to stand at room temperature for 15 hours. The mixture is then poured into ice water, and the solid which forms is collected by filtration, washed with water, and dried. The mixture is chromatographed on neutral alumina, eluting with ether:hexane, to yield l7B-acetoxy-l9- norandrosta-4,9 10) -dien-3 5-01.

Repeating this sequence of procedures with other 19- norandrosta 4,5(10) dien 17/3 o1 3 ones and 19- norandrosta 4,5 (10),l1 trien 17B ol 3 ones having hydrogen and lower alkyl groups at C-17a and hydrogen or methyl groups at 0-18 yields the corresponding 35- hydroxy-lh-ester compounds. e.g.,

1 6 17u-propyl-17p-acetoxy-18-methyl-19-norandrosta- 4,9 1'0) -dien-3 18-01, 17fi-acetoxy-19-norandrosta-4,9 10) -dien-3 3-01, 17,8-acetoxy-lS-methyl-19-norandrosta-4,9( 10)-dien- 3p-0l, 17ot-methyl-17,9-acetoxy-19-norandrosta-4,9( 10) -dien 3,8-01, 17a,18-dimethyl-17fl-acetoxy-19-norandrosta-4,9 10

dien-3 fi-ol, 17a-ethyl-17fl-acetoxy-19-norandrosta-4,9 10 -dien- 35-01, 17 a-ethyl- 1 7,8-acetoxy-1 8-methyl- 19-norandrosta- 4,9 10) -dien-3 5-01, 17p-acetoxy-l S-methyl-19-norandrosta-4,9( l0 ,1 1-

trien-3 301, 17fl-acetoxy-19-norandrosta-4,9 10) ,1 l-trien-Bfl-ol, 17a-methyl-17fl-acetoxy-19-norandrosta-4,9 10) ,1 1-

trien-3,8-ol, 17oz, 18-dimethyl-17p-acetoxy-19-norandrosta-4,9 10) 1 1-trien-3fl-ol, 17a-ethyl-17fl-acetoxy-18-methyl-19-norandrosta- 4,9 10) 1 1-trien-3fl-ol, 17a-ethyl-17fi-acetoxy-19-norandrosta-4,9(10),11-

trien-3 8-01, and the like.

EXAMPLE l7 Repeating the procedure of Example 1 but replacing 501,19 norandrost 17,8 o1 3 one with 17,9 acetoxy- 19 norandrosta 4,9(10) dien 3B ol-3;9 (5,6- dihydro 2H pyran 4' yloxy) 17,9 acetoxy 19- norandrosta 4,9(10) diene is obtained. Similarly, substituting the other products of Example 16 in this procedure, the corresponding 3.13-ethers are obtained, e.g.,

3p (5',6' dihydro 2H pyran 4' yloxy) cpropyl 17p acetoxy 18 methyl 19 norandrosta- 4,9 10)-diene,

3,3 (5',6' dihydro 2H pyran 4' yloxy) 17B- acetoxy-19-norandrosta-4,9 10 -diene,

3,8 (5,6' dihydro 2H pyran 4' yloxy) 17f acetoxy-l S-methyl-19-norandrosta-4,9 10 -diene,

3 3 (5',6' dihydro 2H pyran 4' yloxy) 17amethyl-17fl-acetoxy-19-norandrosta-4,9 10 -diene,

3.5 (5',6' dihydro 2H pyran 4' yloxy) 1701,18- dimethyl-17fi-acetoxy-19-norandrosta-4,9 10)-diene,

3,8 (5',6 dihydro 2H pyran 4' yloxy) 170cethyl-17 3-acetoxy-19-norandrosta-4,9( 10 -diene,

3p (5',6' dihydro 2H pyran 4' yloxy) 17aethyl acetoxy 18 methyl 19 norandrosta- 4,9( 10)-diene,

3B (5,6' dihydro 2H pyran 4 yloxy) 17B- acetoxy 18 methyl 19 norandrosta 4,9(10),11- triene,

318 (5',6' dihydro 2H pyran 4' yloxy) 17pacetoxyl 9-norandrosta-4,9 10) ,1 l-triene,

3,8 (5',6 dihydro 2H pyran 4 yloxy) 17amethyl 17B acetoxy 19 norandrosta 4,9(10),11- triene,

3p (5',6 dihydro 2H pyran 4' yloxy) 1701,18-

dimethyl 17B acetoxy 19 norandrosta 4,9(10), ll-triene,

3B (516 dihydro 2H pyran 4' yloxy) 17aethyl 17,8 acetoxy 18 methyl 19 norandrosta- 4,9 10) ,1 l-triene,

3B (5',6 dihydro 2H pyran 4 yloxy) 17aethyl 17,8 acetoxy 19 norandrosta 4,9(10),11- triene, and the like.

EXAMPLE 18 A solution of 1 g. of 3 3-'(5',6-'dihydro-2H-pyran-4'- yloxy) 17a ethyl 17,8 acetoxy 19 norandrosta- 4,9(10)-diene in 50 m1. of methanol is heated at reflux for three hours with a solution of potassium hydroxide in 1 ml. of water. The reaction mixture is then poured into ice water and the solid which forms is collected by filtration, washed with water to neutrality, and dried to yield 35 (5,6' dihydro 2H pyran 4 yloxy) 170tethyl 19 norandrosta 4,9(10) dien 175- 01 which is recrystallized from methylene chloride: ether.

Similarly, the other 175-ester products of Example 17 are converted to the corresponding 175-01s by this procedure, e.g., 35 (5,6' dihydro 2H pyran 4 yloxy)- 17a methyl 19 norandrosta 4,9(10),11 trien 175- 01, etc.

EXAMPLE 19 Repeating the procedure of Example 14 but replacing 175 (5',6' dihydro 2H pyran 4' yloxy) l9- norandrosta 4,9(10) dien 3 one with 19 norandrosta 4,9(10) diene 17,5 ol 3 one19-norandrosta- 4,9(l)-diene-35,l75-diol is obtained. Then repeating the procedure of Example 1 but replacing a,19-norandrosta- 175 ol 3 one with 19 norandrosta 4,9() diene- 35,175-diol and using 4 ml. instead of 2 ml. of 4-methoqty 5',6' dihydro 2H pyran-35,l75-bis(5',6'- dihydro 2H pyran 4' yloxy) 19 norandrosta- 4,9(l0)-diene is obtained.

Repeating this sequence of procedures with other 19- norandrosta 4,9(10) dien 175 ol 3 ones and 19- norandrosta 4,9(1'0),1l trien 175 o1 3 ones having hydrogen and lower alkyl '(e.g. methyl, ethyl) groups at Cl70t and hydrogen or methyl at C-18 yields the corresponding 35,175 bisethers, e.g., 35,175 bis (5',6' dihydro 2H pyran 4' yloxy) 1700 methylandrosta- 4,9(10) diene, 35,175 bis(5',6 dihydro 2H pyran- 4' yloxy) 1700,18 dimethyl 19 norandrosta 4,9 (10),11-triene, and the like.

The invention claimed is:

1. A 5', 6-dihydro-2H-pyran-4'-yl steroid ether selected from the group consisting of (a) a member selected from the group consisting of 175 (5',6' dihydro 2H pyran 4' yloxy) 5aandrostan-3-ones and 175-(5',6-dihydro-2H-pyran- 4-yloxy)-50t,19-norandrostan-3-ones having at positions (3-200 and 0-406, members selected from the group consisting of hydrogen and methyl, and at position C17u, members selected from the group consisting of hydrogen and lower alkyl;

(b) a member selected from the group consisting of 175 (5',6' dihydro 2H pyran 4' yloxy) androst-4-en-3-ones and 175-(5',6'-dihydro-2H-pyran-4-yl0xy)-l9-norandrost-4-en-3-ones having at position C-4oc, a member selected from the group consisting of hydrogen and chloro; at position C-7OL, a member selected from the group consisting of hydrogen, methyl, fiuoro, and chloro; and at position C-17t1, a member selected from the group consisting of hydrogen and lower alkyl;

(c) a member selected from the group consisting of 175 (5',6' dihydro 2H pyran 4' yloxy) androsta-3,5-dienes and 175-(5',6'-dihydro-2H-pyran- 4-yloxy)-19-norandrosta-3,5-dienes having at position 03, a member selected from the group consisting of lower alkoxy and lower cycloalkoxy; at position C-l7a, a member selected from the group consisting of hydrogen and lower alkyl; and at C-18, a member selected from the group consisting of hydrogen and methyl;

((1) a 175-(5',6-dihydro-2H-pyran-4'-yloxy)-50t-androst-l-en-3-one having at positions C1 and C2, members selected from the group consisting of hydrogen and methyl, at least one of said members at C1 and C-2 being methyl; and at position 0-1700, a member selected from the group consisting of hydrogen and lower alkyl;

(e) a member selected from the group consisting of androst-4-enes and l9-norandrost-4-enes having at position C3, a member selected from the group consisting of keto, hydrogen, hydroxy, conventional hydrolyzable esters of said hydroxy and 5',6-dihydro- 2H-pyran-4'-yloxy; between positions C6 and C7, :1

bond selected from the group consisting of single and double bonds; at position C6, first and second members selected from the group consisting of hydrogen, methyl, fluoro, and chloro, said second member being present only when the bond between C6 and C7 carbons is a single bond; at position Ct, a member selected from the group consisting of hydrogen and lower alkyl; at position C-175, a member selected from the group consisting of hydroxy, conventional hydrolyzable esters of said hydroxy, and 5,6'-dihydro-2H-pyran-4-yloxy and at least one of said C-3 and C- positions having said 5,6-dihydro-2H-pyran-4-yloxy group; and at position C- 18, a member selected from the group consisting of hydrogen and methyl;

(f) a 19-norandrosta-4,9(10-)-diene having at position C3, a member selected from the group consisting of keto, hydrogen, hydroxy, conventional hydrolyzable esters of said hydroxy, and 5',6-dihydro-2H-pyran- 4'-yloxy between carbons at C11 and C12, a member selected from the group consisting of single and double bonds; at position C170t, a member selected from the group consisting of hydrogen and lower alkyl; at position C175, a member selected from the group consisting of hydroxy, conventional hydrolyzable esters of said hydroxy, and 5',6'-dihydro-2H- pyran-4-yloxy and at least one of said C3 and C- 175 positions having said 5',6'-dihydro-2H-pyran-4'- yloxy; and at position C-18, a member selected from the group consisting of hydrogen and methyl.

2. The steroid ether of claim 1 wherein the ether is a member selected from the group consisting of 175-(5',6- dihydro-2H-pyran-4'-yloxy)-5'0t-androstan-3-ones and 175- (5,6' dihydro 2H pyran 4' yloxy) 50,19 norandrostan-3-0nes having at positions C-2a and C--40t, members selected from the group consisting of hydrogen and methyl, and at position C-1700, a member selected from the group consisting of hydrogen and lower alkyl.

3. The steroid ether of claim 2 wherein the ether is 20: methyl 175 (5',6' dihydro 2H pyran-4'-yloxy)- 50t-androstan-3-one.

4. The steroid ether of claim 2 wherein the ether is 40 methyl 175 (5',6 dihydro 2H pyran-4'-yloxy)- SOL-3IldIOStflIl-3-OI'1G.

5. The steroid ether of claim 1 wherein the ether is a member selected from the group consisting of 175-(5,6'- dihydro-2H-pyran-4-yloxy)androst-4-en-3-ones and 175- (5',6'-dihydro 2H pyran 4 yloxy) 19 norandrost- 4-en-3-ones having at position C40t, a member selected from the group consisting of hydrogen or chloro; at position C7, a member selected from the group consisting of hydrogen, methyl, fiuoro, and chloro; and at position C- 170, a member selected from the group consisting of hydrogen and lower alkyl.

6. The steroid ether of claim 5 wherein the ether is 175- 5 ,6-dihydro-2H-pyran-4-yloxy) androst-4-en-3-one.

7. The steroid ether of claim 5 wherein the ether is 4 chloro 175 (5',6 dihydro 2H pyran 4' yloxy) androst-4-en-3-one.

8. The steroid ether of claim 5 wherein the ether is 700,170; dimethyl 175 (5',6' dihydro 2H pyran 4'- yloxy)-19-norandrost-4-en-3-one.

9. The steroid ether of claim 5 wherein the ether is 175 (5,6' dihydro 2H pyran 4' yloxy) 19 norandrost-4-en-3-one.

10. The steroid ether of claim 5 wherein the ether is 4-chloro 175 (5',6' dihydro-2H-pyran-4'-yloxy)-19 norandrost-4-en-3-one.

11. The steroid ether of claim 5 wherein the ether is 70t-methyl 175 (5',6 dihydro-2H-pyran-4'yloxy)-19- nordandrost-4-en-3-one.

12. The steroid ether of claim 1 wherein the ether is a member selected from the group consisting of 175- (5',6-dihydro-2H-pyran 4' yloxy)androsta 3,5-dienes and 175-(5 ',6'-dihydro 2H-pyran-4-yloxy)-19-norandro- 19 sta-3,5-dienes having at position C-3, a member selected from the group consisting of lower alkoxy and lower cycloalkoxy; at position C17oz, a member selected from the group consisting of hydrogen and lower alkyl; and at C-18, a member selected from the group consisting of hydrogen and methyl.

13. The steroid ether of claim 12 wherein the ether is 3-cyclopentoxy-17a methyl 175 (5',6' dihydro-2H- pyran-4'-yloxy)-l9-norandrosta-3,S-diene.

14. The steroid ether of claim 12 wherein the ether is 3 cyclopentoxy 170:,18 dimethyl-17}3-(5',6'-dihydro- 2H-pyran-4'-yloxy)-19-norandrosta-3,5-diene.

15. The steroid ether of claim 12 wherein the ether is 3-methoXy-17a,18-dimethyl-17B (5,6' dihydro 2H- pyran-4'-yloxy) -19-norandrosta-3 ,5 -diene.

16. The steroid ether of claim 1 wherein the ether is a 17 3 (5',6' dihydro-ZI-I-pyran 4' yloxy) 5a androst- 1-en-3-one having at positions C1 and C2, members selected from the group consisting of hydrogen and methyl, at least one of said members at C1 and C2 being methyl and at a position C-17a, a member selected from the group consisting of hydrogen and lower alkyl.

17. The steroid ether of claim 16 wherein the ether is l-methyl 17;? (5,6-dihydro 2H pyran-4'-yloxy)4ixandrost-1-en-3-one.

18. The steroid ether of claim 16 wherein the ether is 2-methyl-l7,8-(5,6'-dihydro 2H pyran 4' yloxy)- 5a-androst-1-en-3-one.

19. The steroid ether of claim 16 wherein the ether is 2,17a-dimethyl 17fi-(5,6' dihydro-2H pyran-4-yloxy)- 5a-androst-1-en-3-one.

20. The steroid ether of claim 1 wherein the ether is selected from the group consisting of androst-4-enes and 19-norandrost-4-enes having at position C-3, a member selected from the group consisting of keto, hydrogen, hydroxy, conventional hydrolyzable esters of said hydroxy and 5',6-dihydro-2H-pyran-4-yloxy; between positions -6 and C7, a bond selected from the group consisting of single and double bonds; at position C-6, first and second members selected from the group consisting of hydrogen, methyl, fiuoro, and chloro, said second member being present only when the bond between the C-6 and C7 carbons is a single bond; at C17u, a member selected from the group consisting of hydrogen and lower alkyl; at C-17 3, a member selected from the group consisting of hydroxy, conventional hydrolyzable esters of said hydroxy, and ',6'-dihydro-2H-pyran-4'-yloXy and at least one of said 03 and C-17 s positions having said 5,6'- dihydro-2H-pyran4-yloxy group; and at position C18, a member selected from the group consisting of hydrogen and methyl groups.

21. The steroid ether of claim wherein the ether is 17u-methyl 17,9-(5,6' dihydro-ZI-I-pyran 4' yloxy)- 19-norandrost-4-en-3-one.

22. The steroid ether of claim 20 wherein the ether is 3/3 acetoxy Uni-methyl 173 (5,6'-dihydro-2H-pyran- 4'-yloxy)-19-norandrost-4-ene.

23. The steroid ether of claim 20 wherein the ether is 17a,18-dimethyl-17fl-(5',6'-dihydro-2Hpyran 4'-yloxy)- 19-n0randrost-4-en-3-one.

24. The steroid ether of claim 20 wherein the ether is 3-acetoxy-17a,18 dimethyl 17,9 (5,6'-dihydr0-2H- pyran-4'-y1oxy) -19-norandrost-4-ene,

25. The steroid ether of claim 20 wherein the ether is 6a-fluOIO-l7oc -methyl 17B-(5',6' dihydro-2H-pyran-4'- yloxy)-19-norandrost-4-en-3-one.

26. The steroid ether of claim 20 wherein the ether is 6a-fluOlO-l7a,l8 dimethyl l7fl-(5,6' dihydro-2H- pyran-4'-yloxy) l9-norandrost-4-en-3-one.

27. The steroid ether of claim 20 wherein the ether is 6a,l7a-dimethyl-l7fi-(5',6'-dihydro-2H-pyran 4'-yloxy)- 19-norandrosta-4,6-dien-3-one.

28. The steroid ether of claim 20 wherein the ether is 6oc ,l 8-dimethyl-17aethyl-17/3-(5',6-dihydro-2H-pyran 4- yloxy)-19-norandrosta-4,6-dien-3-one.

29. The steroid ether of claim 20 wherein the ether is 3-(5',6-dihydro-2H-pyran-4-yloxy) 17oz methyl-19- norandrost-4-en-l7B-ol.

30. The steroid ether of claim 20 wherein the ether is 3-(5,6'-dihydro-2H-pyran-4'-yloxy)-17 x-rnethyl 17B- acetoxy-19-norandrost-4-ene.

31. The steroid ether of claim 20 wherein the ether is 3 ,17,B'-bis(5',6'-dihydro-2H-pyran-4'-yloxy)-17a-methyl- 19-norandrost-4-ene.

32. The steroid ether of claim 1 wherein the ether is a 19-norandrosta-4,9(10)-diene having at position C3, a member selected from the group consisting of keto, hydrogen, hydroxy, conventional hydrolyzable esters of said hydroxy, and 5,6'-dihydro-2H-pyran-4'-yloxy; between carbons at C-11 and C12, a member selected from the group consisting of single and double bonds; at position Cl7oc, a member selected from the group consisting of hydrogen and lower alkyl; at position C-175, a member selected from the group consisting of hydroxy, conventional hydrolyzable esters of said hydroxy, and 5',6-di hydro-2H-pyran-4'-yloxy, and at least one of said C3 and C17B positions having said 5',6-dihydro-2H-pyran-4- yloxy group; and at position C-18, a member selected from the group consisting of hydrogen and methyl.

33. The steroid ether of claim 32 wherein the ether is 3(3-(5',6'-dihydro-2H-pyran-4'-yloxy) 17oz ethyl 19- norandrosta-4,9( 10 -dien- 175-01.

34. The steroid ether of claim 32 wherein the ether is 17B-(5',6'-dihydro-2H-pyran-4-yloxy) 19 norandrosta-4,9( 10),11-trien-3-one.

35. The steroid ether of claim 32 wherein the ether is a methyl 17B-(5',6 dihydro 2H pyran-4'-yloxy)- 19-norandrosta-4,9(10),1 1-trien-3-one.

36. The steroid ether of claim 32 wherein the ether is 3B-(5,6'-dihydro-2I-I-pyran-4'-yloxy)-17u methyl-19- norandrosta-4,9 10) ,1 1-trien-17fi-ol.

References Cited UNITED STATES PATENTS 3,294,786 12/1966 Cross et al. 260-23955 3,313,808 4/1967 de Ruggieri et al. 260239.55 3,326,903 6/1967 Klimstra 260239.55 3,338,925 8/1967 Fried 260397.4 3,352,853 11/1967 Kli'mstra 260239.55

HENRY A. FRENCH, Primary Examiner U.S. c1. X.R.

UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION patent 3, 525, 740 Dated August 25, 1970 Inventor(s) Alexander D. Cross and John A. Edwards It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:

' Column 1, line 20, "731,000" should read 731,300

Column 2, lines l-ll, that portion of Formula (V) reading X R .C. i should be Column 4, lines 60-72, that portion of the Formula (XVIII) reading ll ll OIORlZ should be Column 9, line 60, "yloxy,-" should read yloxy)- Column 10, line 33, "4, 6-176- should read 4,6-dien- 176- Column 13, line 5, "xyloxy" should read yloxy and line 21, "acetoxy-8-methylandrost" should read Iii-methylandrosta Column 19, line 24, "4a" should read 504 Column 20, line 32, "5 ,6" should read 5 ,6

Signed and sealed this 1 8th day of July 1972.

(SEAL) Attest:

EDWARD M.FLETCHER,JR. ROBERT GOTTSCHALK Attesting Officer Commissioner of Patents 

